首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >Alectinib for Patients with ALK Rearrangement–Positive Non–Small Cell Lung Cancer and a Poor Performance Status (Lung Oncology Group in Kyushu?1401)
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Alectinib for Patients with ALK Rearrangement–Positive Non–Small Cell Lung Cancer and a Poor Performance Status (Lung Oncology Group in Kyushu?1401)

机译:alectinib用于患有ALK重排阳性非小细胞肺癌的患者及性能状况不佳(九州肺部肿瘤组织?1401)

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Abstract Introduction Alectinib has shown marked efficacy and safety in patients with anaplastic lymphoma receptor tyrosine kinase gene ( ALK ) rearrangementpositive NSCLC and a good performance status (PS). It has remained unclear whether alectinib might also be beneficial for such patients with a poor PS. Methods Eligible patients with advanced ALK rearrangementpositive NSCLC and a PS of 2 to 4 received alectinib orally at 300 mg twice daily. The primary end point of the爏tudy was objective response rate (ORR), and the most爄nformative secondary end point was rate of PS improvement. Results Between September 2014 and December 2015, 18 patients were enrolled in this phase II study. Of those patients, 12, five, and one had a PS of 2, 3, or 4, respectively, whereas four patients had received prior crizotinib treatment. The ORR was 72.2% (90% confidence interval: 52.985.8%). The ORR did not differ significantly between patients with a PS of 2 and those with a PS of 3 or higher (58.3% and 100%, respectively [ p ? 0.114]). The PS improvement rate was 83.3% (90% confidence interval: 64.893.1%, p 0.0001), with the frequency of improvement to a PS of 0 or 1 being 72.2%. The median progression-free survival was 10.1 months. Toxicity was mild, with the frequency of adverse events of grade 3 or higher being low. Neither dose reduction nor withdrawal of alectinib because of toxicity was necessary. Conclusions Alectinib is a treatment option for patients with ALK rearrangementpositive NSCLC and a poor PS.
机译:摘要简介alectinib显示了促进淋巴瘤受体酪氨酸激酶基因(ALK)重新排列阳性NSCLC患者的显着疗效和安全性和良好的性能状态(PS)。它仍然尚不清楚莱切韦是否可能对贫穷PS的患者有益。方法符合先进的ALK重新排列阳性NSCLC患者的患者2至4的PS,每天两次以300毫克口服邻接莱切韦。爏tudy的主要终点是客观响应率(ORR),最多的Nformative次要终点是PS改善的速率。结果2014年9月至2015年12月,18例患者参加了本II期研究。其中12,5和一个患者分别为2,3或4个,而4名患者已收到先前的蠕动治疗。 ORR为72.2%(90%置信区间:52.985.8%)。患者在患者的2个患者中没有显着差异,PS的PS为3或更高(分别为58.3%和100%[p≤0.114])。 PS改善率为83.3%(90%置信区间:64.893.1%,P <0.0001),改善0或1的频率为72.2%。中位进展生存期为10.1个月。毒性是温和的,频率不良事件的3级或更高的低。需要由于毒性而减少的剂量减少也不撤离莱切韦。结论alectinib是ALK重新排列阳性NSCLC和贫患者患者的治疗选择。

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